Label: UP AND UP ALLERGY RELIEF- fexofenadine hydrochloride tablet, film coated
- NDC Code(s): 11673-617-00, 11673-617-01, 11673-617-22, 11673-617-39, view more
- Packager: Target Corporation
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated September 30, 2021
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- Official Label (Printer Friendly)
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Active ingredient (in each tablet) Fexofenadine HCl 180 mg
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Purpose Antihistamine
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Uses temporarily relieves these symptoms due to hay fever or other upper respiratory allergies: • runny nose - • itchy, watery eyes - • sneezing - • itching of the nose or throat
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Warnings Do not use - if you have ever had an allergic reaction to this product or any of its ingredients. Ask a doctor before use if you have - kidney disease. Your doctor should determine if you ...
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Directions adults and children 12 years of age and over - take one 180 mg tablet with water once a day; do not take more than 1 tablet in 24 hours - children under 12 years of age - do not ...
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Other information • do not use if printed blister unit is broken or torn - • store between 20° -25°C (68° -77°F) • protect from excessive moisture - • this product meets the requirements of USP Dissolution Test ...
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Inactive ingredients colloidal silicon dioxide, croscarmellose sodium, FD&C blue #2 aluminum lake, FD&C red #40 aluminum lake, FD&C yellow #6 aluminum lake, lactose monohydrate, magnesium stearate, microcrystalline ...
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Questions? Call 1-888-547-7400
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Package/Label Principal Display Panel Compare to active ingredient in Allegra® Allergy - non-drowsy - allergy relief - fexofenadine hydrochloride tablets 180 mg/antihistamine - indoor/outdoor allergy relief - • sneezing - • runny nose - • itchy ...
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INGREDIENTS AND APPEARANCEProduct Information
